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Neurology|June 15, 2007
Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the familiesA J van der Kooi, W S Frankhuizen, P G Barth, et al.
Journal of Neuroimmunology|July 23, 2008
The Lambert-Eaton myasthenic syndrome 1988-2008: a clinical picture in 97 patientsM J Titulaer, P W Wirtz, J B M Kuks, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 14, 2013
Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapyJ C van den Bergen, S M Schade van Westrum, L Dekker, et al.
Neurology|September 1, 1996
Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth diseaseA A Gabreëls-Festen, J E Hoogendijk, P H Meijerink, et al.
Antimicrobial Agents and Chemotherapy|June 27, 2026
Pyocyanin produced by Pseudomonas aeruginosa creates legacy effects that promote antibiotic resistance evolution in enterococciM G J de Vos, V Jansen, O El Bouhlali, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 20, 2002
Difference in distribution of muscle weakness between myasthenia gravis and the Lambert-Eaton myasthenic syndromeP W Wirtz, M Sotodeh, M Nijnuis, et al.
Neurology|May 16, 2007
Phenotype of Charcot-Marie-Tooth disease Type 2H M E Bienfait, F Baas, J H T M Koelman, et al.
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